Skip to main content
Log in

Effects of endurance training on myosin heavy-chain isoforms and enzyme activity in the rat diaphragm

  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

We investigated the effects of endurance training (20 m/min, 60 min/day, 5 days/week) on myosin heavy-chain (MHC) isoforms and succinic dehydrogenase (SDH) activity in rat crural and costal diaphragms, and plantaris muscles. Although the 4-week endurance training produced significant (P<0.05) increases, both in SDH activity and the percentage of isoform HCIIa in the plantaris of the trained rat compared with the sedentary control rat, these alterations did not occur in either the crural or costal diaphragms. After 10 weeks of endurance training, trained animals had significantly (P<0.05) higher SDH activity in the costal diaphragm and the plantaris. Moreover, a significant (P<0.05) decrease occurred in the percentage of HCIIb in the costal diaphragm, and a significant (P<0.01) decrease in the percentage of HCIIb concomitant with a significant (P<0.05) increase of HCIIa resulted in the plantaris. However, the crural diaphragm did not show any significant changes after 10 weeks of endurance training. These results indicate that endurance training induces an alteration in the expression of an MHC phenotype, in addition to causing an increase in oxidative enzyme activity. However, the alterations in response to endurance training are apparently not uniform, varying between regions and/or kinds of muscles.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Akabas SR, Bazzy AR, DiMauro S, Haddad GG (1989) Metabolic and functional adaptation of the diaphragm to training with resistive loads. J Appl Physiol 66:529–535

    Google Scholar 

  2. Bär A, Pette D (1988) Three fast myosin heavy chains in adult rat skeletal muscle. FEBS Lett 235:153–155

    Google Scholar 

  3. Billeter R, Heizmann CW, Howald H, Jenny E (1981) Analysis of myosin light and heavy chain types in single human skeletal muscle fibers. Eur J Biochem 116:389–395

    Google Scholar 

  4. Brooks GA, White TP (1978) Determination of metabolic and heart rate responses of rats to treadmill exercise. J Appl Physiol 45:1009–1015

    Google Scholar 

  5. Burke RE, Edgerton VR (1975) Motor unit properties and selective involvement in movement. Exercise Sport Sci Rev 3:31–81

    Google Scholar 

  6. Cooperstein SJ, Lazarow A, Kurfess NJ (1950) A microspectrophotometric method for the determination of succinic dehydrogenase. J Biol Chem 186:129–139

    Google Scholar 

  7. Crosfill ML, Widdicombe JG (1961) Physical characteristics of the chest and lungs and the work of breathing in different mammalian species. J Physiol (Lond) 158:1–14

    Google Scholar 

  8. DeTroyer A, Sampson M, Sigrist S, Macklem PT (1981) The diaphragm: two muscles. Science 213:237–238

    Google Scholar 

  9. Edwards RHT, Faulkner JA (1985) Structure and function of the respiratory muscles. In: Roussos C, Macklem PT (eds) The thorax, chapter 9, part A. Dekker, New York, pp 297–326

    Google Scholar 

  10. Farkas GA, Roussos C (1982) Adaptability of the hamster diaphragm to exercise and/or emphysema. J Appl Physiol 53:1263–1272

    Google Scholar 

  11. Fitzsimons DP, Diffee GM, Herrick RE, Baldwin KM (1990) Effects of endurance exercise on isomyosin patterns in fastand slow-twitch skeletal muscles. J Appl Physiol 68:1950–1955

    Google Scholar 

  12. Fregosi RF, Sanjak M, Paulson DJ (1987) Endurance training does not affect diaphragm mitochondrial respiration. Respir Physiol 67:225–237

    Google Scholar 

  13. Gollnick PD, Armstrong RB, Saltin B, Saubert CW IV, Sembrowich WL, Shepherd RE (1973) Effect of training on enzyme activity and fiber composition of human skeletal muscle. J Appl Physiol 34:107–111

    Google Scholar 

  14. Günther PG (1953) Das muskuläre Substrat der Bewegungsund Halteleist-ung des menschlichen Zwerchfells. Acta Anat 17:348–352

    Google Scholar 

  15. Holloszy JO, Booth FW (1976) Biochemical adaptations to endurance exercise in muscle. Annu Rev Physiol 38:273–291

    Google Scholar 

  16. Keith A (1905) The nature of the mammalian diaphragm and pleural cavities. J Anat Physiol 39:243–284

    Google Scholar 

  17. Metzger JM, Scheidt KB, Fitts RH (1985) Histochemical and physiological characteristics of the rat diaphragm. J Appl Physiol 58:1085–1091

    Google Scholar 

  18. Monges H, Salducci J, Naudy B (1978) Dissociation between the electrical activity of the diaphragmatic dome and crural muscular fibers during esophageal distention, vomiting and eructation. An electromyographic study in the dog. J Physiol (Paris) 74:541–554

    Google Scholar 

  19. Moore RL, Gollnick PD (1982) Response of ventilatory muscles of the rat to endurance training. Pflügers Arch 392:268–271

    Google Scholar 

  20. Pette D, Müller W, Leisner E, Vrbová G (1976) Time dependent effects on contractile properties, fibre population, myosin light chains and enzymes energy metabolism in intermittently and continuously stimulated fast twitch muscles of the rabbit. Pflügers Arch 364:103–112

    Google Scholar 

  21. Powers SK, Lawler J, Criswell D, Dodd S, Grinton S, Bagby G, Silverman H (1990) Endurance-training-induced cellular adaptations in respiratory muscles. J Appl Physiol 68:2114–2118

    Google Scholar 

  22. Powers SK, Lawler J, Criswell D, Silverman H, Forster HV, Grinton S, Harkins D (1990) Regional metabolic differences in the rat diaphragm. J Appl Physiol 69:648–650

    Google Scholar 

  23. Sieck GC, Fournier M (1989) Diaphragm motor unit recruitment during ventilatory and nonventilatory behaviors. J Appl Physiol 66:2539–2545

    Google Scholar 

  24. Sieck GC, Cheung T, Blanco CE (1991) Diaphragm capillarity and oxidative capacity during postnatal development. J Appl Physiol 70:103–111

    Google Scholar 

  25. Sugita H, Okumura Y, Ayai K (1969) Application of a property of troponin to determination of tropomyosin content of a small piece of muscle. J Biochem (Tokyo) 65:971–972

    Google Scholar 

  26. Sugiura T, Murakami N (1990) Separation of myosin heavy chain isoforms in rat skeletal muscles by gradient sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Biomed Res 11:87–91

    Google Scholar 

  27. Sugiura T, Morimoto A, Sakata Y, Watanabe T, Murakami N (1990) Myosin heavy chain isoform changes in rat diaphragm are induced by endurance training. Jpn J Physiol 40:759–763

    Google Scholar 

  28. Termin A, Staron RS, Pette D (1989) Myosin heavy chain isoforms in histochemically defined fiber types of rat muscle. Histochemistry 92:453–457

    Google Scholar 

  29. Termin A, Staron RS, Pette D (1989) Changes in myosin heavy chain isoforms during chronic low-frequency stimulation of rat fast hindlimb muscles. A single-fiber study. Eur J Biochem 186:749–754

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sugiura, T., Morimoto, A. & Murakami, N. Effects of endurance training on myosin heavy-chain isoforms and enzyme activity in the rat diaphragm. Pflügers Arch 421, 77–81 (1992). https://doi.org/10.1007/BF00374736

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00374736

Key words

Navigation